At a Glance
- Tasks: Lead safety data reviews and drive risk management strategies for patient safety.
- Company: Join Bristol Myers Squibb, a leader in innovative pharmaceuticals.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Dynamic team environment with a commitment to innovation and collaboration.
- Why this job: Make a real impact on patient safety while working with cutting-edge technologies.
- Qualifications: 4-6+ years in pharmacovigilance and a scientific degree required.
The predicted salary is between 80000 - 100000 £ per year.
Overview
Bristol Myers Squibb is seeking a talented pharmacovigilance professional to join the Safety Science team as Senior Manager, Patient Safety Science.
You'll be at the heart of how BMS characterises and protects the safe use of its medicines, working closely with Medical Safety Assessment Physicians and Safety Management Teams to own signal detection, lead safety data review meetings, drive risk management strategies, and ensure robust pharmacovigilance compliance across the product lifecycle-from early development through postmarketing.
Responsibilities
- Detect and Manage Signals - Lead quantitative signal detection, author comprehensive signal reports, and escalate issues that could impact key safety milestones.
- Drive Safety Surveillance - Prepare and contribute to aggregate safety documents (DSURs, PBRERs, PADERs) and respond to health authority queries.
- Support Clinical Development - Contribute to safety sections of protocols, investigator brochures, CSRs, and informed consent forms.
- Shape Regulatory Submissions - Author safety sections of MAAs, including ISS, SCS, clinical overviews, and product labelling (USPI, CCDS, Sm PC).
- Lead Risk Management - Develop and maintain global and EU Risk Management Plans, additional Risk Minimisation Measures, and Post-Authorisation Safety Studies.
- Champion Innovation - Leverage AI, automation, and digital platforms to continuously improve safety workflows and data analysis.
Qualifications
- Education: Scientific degree (BS, MS, Pharm D, Ph D, MD, RN, or equivalent).
- Experience: 4-6+ years in pharmacovigilance, drug development, or the pharmaceutical industry.
- Skills & Attributes: Solid grounding in global pharmacovigilance regulations and postmarketing safety requirements; strong analytical mindset; excellent organizational skills; collaborative, adaptable communicator; comfortable working with emerging technologies including AI and digital safety tools.
- Work Model & Accessibility
BMS has an occupancy structure that determines where an employee is required to conduct their work.
Roles may be site-essential (onsite 100%), site-by-design (hybrid with at least 50% onsite), or field-based/remote-by-design (travel may be required).
For field-based and remote-by-design roles, the ability to travel to visit customers, patients or partners and to attend meetings is an essential job function.
Equal Opportunity & Accessibility
BMS is committed to equal employment opportunity and providing reasonable workplace accommodations.
If you require accommodations in completing this application or during the recruitment process, please contact .
- For our full EEO statement, visit
- Data Privacy
Data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
We will never request payments or sensitive information during recruitment.
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